Class II ยท Moderate risk
Cardiogen-82
GMP deviation; Sr-82 levels exceeded alert limit specification
National Drug Code
Is NDC 0270-0091-01 recalled?
CardioGen-82 · 1 INJECTION, SOLUTION in 1 PACKAGE (0270-0091-01)
Yes — this exact package was recalled
1 FDA recall names the code 0270-0091-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Rubidium Chloride RB-82
- Strength
- RUBIDIUM CHLORIDE RB-82 150 mCi/1
- Form
- Injection, Solution · Intravenous
- Labeler
- Bracco Diagnostics Inc
- Type
- Human Prescription Drug
- Product code
- 0270-0091
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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